According to the research I've done, Prader-Willi Syndrome is rarely a result of translocation, but it is a possibility. Translocation in this syndrome results in an inactivation of genes on the paternal chromosome 15.
A translocation chromosomal mutation will result when two non-homologous chromosomes each broken by some sort of clastogen and then are swapped.
Translocation
Translocations can result into gene dysregulation, thus leading to diseases like cancer.
none. its a slight mutation in 23rd x chromosome
No. It arises due to point mutations (like A -> T).
There is no "cure" for haemophilia, only treatment with the appropriate clotting factors.
Leaching is another word for translocation.
translocation!
translocation
This condition is referred to as chromosomal translocation.
Haemophilia (also spelled hemophilia) is genetic disorder. It is more licely for a male to get it than female. About one of 5,000-10,000 male babies are born with Haemophilia A. About one of 20,000-34,000 male babies are born with Haemophilia B.